dc.contributor.author
Jowett, Laura A.
dc.contributor.author
Howe, Ethan N. W.
dc.contributor.author
Soto Cerrato, Vanessa
dc.contributor.author
Van Rossom, Wim
dc.contributor.author
Pérez Tomás, Ricardo E.
dc.contributor.author
Gale, Philip A.
dc.date.issued
2018-11-07T16:23:06Z
dc.date.issued
2018-11-07T16:23:06Z
dc.date.issued
2017-08-24
dc.date.issued
2018-11-07T16:23:06Z
dc.identifier
https://hdl.handle.net/2445/125895
dc.description.abstract
Prodigiosin is one of the most potent anion transporters in lipid bilayer membranes reported to date. Inspired by the structure of this natural product, we have recently designed and synthesised a new class of H+/Cl− cotransporters named 'perenosins'. Here we report a new library of indole-based perenosins and their anion transport properties. The new transporters demonstrated superior transmembrane transport efciency when compared to other indole-based transporters, due to favourable encapsulating efects from the substituents on the perenosin backbone. Anion transport assays were used to determine the mechanism of chloride transport revealing that the compounds function as 'strict' HCl cotransporters. Cell viability studies showed that some compounds specifcally trigger lateonset cell death after 72h with a unique correlation to the position of alkyl chains on the perenosins. Further investigations of cell death mechanism showed a mixture of cell cycle arrest and apoptosis was responsible for the observed decrease in cell viability.
dc.format
application/pdf
dc.format
application/pdf
dc.publisher
Nature Publishing Group
dc.relation
Reproducció del document publicat a: https://doi.org/10.1038/s41598-017-09645-9
dc.relation
Scientific Reports, 2017, vol. 7
dc.relation
https://doi.org/10.1038/s41598-017-09645-9
dc.rights
cc-by (c) Jowett, Laura A. et al., 2017
dc.rights
http://creativecommons.org/licenses/by/3.0/es
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Patologia i Terapèutica Experimental)
dc.title
Indole-based perenosins as highly potent HCl transporters and potential anti-cancer agents
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion